Medtronic Reusable Instruments 907347Recalls & reported problems
Medtronic Sofamor Danek, Inc. · CURETTE 907347 SMALL FORWARD ANGLE · Class 1
All models of Medtronic Reusable Instruments (36)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00885074499468), received between Nov 18, 2024 and Jan 21, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (3 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 21, 2026Break
INFORMATION WAS RECEIVED FROM MANUFACTURER REPRESENTATIVE REGARDING PRODUCTS USED FOR SPINAL THERAPY. IT WAS REPORTED THAT WHILE PREPPING FOR SURGERY, THE INSTRUMENTS WERE DROPPED ON FLOOR AND GOT BROKEN. THERE IS NO PATIENT INVOLVED AND NO FURTHER COMPLICATIONS OR SYMPTOMS REPORTED REGARDING THE EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24128385 ↗MalfunctionJan 28, 2025Break; Break
INFORMATION WAS RECEIVED FROM A MANUFACTURER REPRESENTATIVE REGARDING AN INSTRUMENT USE FOR TRANSFORAMINAL LUMBAR INTERBODY FUSION. IT WAS REPORTED THAT THE CUP SNAPPED OFF CURETTE. THERE WAS NO PATIENT INVOLVEMENT REPORTED. THERE WERE NO FURTHER COMPLICATIONS REPORTED REGARDING THE EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21261233 ↗MalfunctionNov 18, 2024Break; Break
INFORMATION WAS RECEIVED FROM A MANUFACTURER REPRESENTATIVE REGARDING A PART USED FOR SPINAL THERAPY. IT WAS REPORTED THAT THE TIP WAS BROKEN. THERE WAS NO FURTHER INFORMATION REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20705711 ↗
Other CURETTE, SURGICAL, GENERAL USE devices
- Sklar Instruments 941-1320Sklar Corporation · CURETTE, SURGICAL, GENERAL USE1 recall0 reports
- Medtronic Reusable Instruments 2900163Medtronic Sofamor Danek, Inc. · CURETTE, SURGICAL, GENERAL USE11 reports
- Medtronic Reusable Instruments 9560547Medtronic Sofamor Danek, Inc. · CURETTE, SURGICAL, GENERAL USE7 reports
- na 2900162Medtronic Sofamor Danek, Inc. · CURETTE, SURGICAL, GENERAL USE3 reports
- Medtronic Reusable Instruments 875-304Medtronic Sofamor Danek, Inc. · CURETTE, SURGICAL, GENERAL USE2 reports
- na 907349Medtronic Sofamor Danek, Inc. · CURETTE, SURGICAL, GENERAL USE1 report
- Medtronic Reusable Instruments 9560546Medtronic Sofamor Danek, Inc. · CURETTE, SURGICAL, GENERAL USE1 report
- Symmetry Surgical 23-1045Aspen Surgical Products, Inc. · Curette, Surgical, General Use1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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